Cri-Du-Chat Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_12580)
External Link https://www.disgenet.org/browser/0/1/0/C0010314
Similar Terms
Downloads & Tools

Genes

10 genes associated with the disease Cri-Du-Chat Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CTNND2 catenin (cadherin-associated protein), delta 2
DNAH5 dynein, axonemal, heavy chain 5
EGR1 early growth response 1
IL33R interleukin 33 receptor
MRPL36 mitochondrial ribosomal protein L36
SEMA5A sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1
TERT telomerase reverse transcriptase
TRPV6 transient receptor potential cation channel, subfamily V, member 6